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Volume 29(1); Feb 2024
Editorial
Commentary on "Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience"
Hye Young Jin
Ann Pediatr Endocrinol Metab. 2024;29(1):1-2.   Published online February 29, 2024
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Review Articles
An overview of growth hormone therapy in pediatric cases documented in the Kabi International Growth Study (Pfizer International Growth Database)
Mitchell E. Geffner, Michael B. Ranke, Michael P. Wajnrajch
Ann Pediatr Endocrinol Metab. 2024;29(1):3-11.   Published online February 29, 2024
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Pediatric and adult osteoporosis: a contrasting mirror
Hanene Lassoued Ferjani, Ines Cherif, Dorra Ben Nessib, Dhia Kaffel, Kaouther Maatallah, Wafa Hamdi
Ann Pediatr Endocrinol Metab. 2024;29(1):12-18.   Published online February 29, 2024
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Original Articles
Association of maternal insulin resistance with neonatal insulin resistance and body composition/size: a prospective cohort study in a sub-Saharan African population
Ibironke J. Akinola, Peter O. Ubuane, Adeyemi O. Dada, Joy O. Chionuma, Taiwo O. Kuku-Kuye, Folasade D. Olalere
Ann Pediatr Endocrinol Metab. 2024;29(1):19-28.   Published online February 29, 2024
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Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience
Su Jin Kim, Eunyoung Joo, Jisun Park, Chang Ahn Seol, Ji-Eun Lee
Ann Pediatr Endocrinol Metab. 2024;29(1):38-45.   Published online February 29, 2024
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Effectiveness and safety of pamidronate treatment in nonambulatory children with low bone mineral density
Myeongseob Lee, Ahreum Kwon, Kyungchul Song, Hae In Lee, Han Saem Choi, Junghwan Suh, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2024;29(1):46-53.   Published online February 29, 2024
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Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2024;29(1):54-59.   Published online February 29, 2024
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Case Report
Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review
Jihyun Ha, Yunha Choi,, Mo Kyung Jung, Eun-Gyong Yoo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2024;29(1):60-66.   Published online February 29, 2024
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Letters to the Editor
Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation
Jiyeon Kim, Eu Seon Noh, Min-Sun Kim, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho
Ann Pediatr Endocrinol Metab. 2024;29(1):67-69.   Published online January 28, 2024
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The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome
Jun Lee, Minji Kim, Sukdong Yoo, Ju Young Yoon, Chong Kun Cheon
Ann Pediatr Endocrinol Metab. 2024;29(1):70-72.   Published online February 29, 2024
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